Development of potent, selective SRPK1 inhibitors as potential topical therapeutics for neovascular eye disease
Serine/arginine-protein kinase 1 (SRPK1) regulates alternative splicing of VEGF-A to pro-angiogenic isoforms and SRPK1 inhibition can restore the balance of pro/antiangiogenic isoforms to normal physiological levels. The lack of potency and selectivity of available compounds has limited development...
| Main Authors: | Batson, Jennifer, Toop, Hamish D., Redondo, Clara, Babaei-Jadidi, Roya, Chaikaud, Apirat, Wearmouth, Stephen F., Gibbons, Brian, Allen, Claire, Tallant, Cynthia, Zhang, Jingxue, Du, Chunyun, Hancox, Jules C., Hawtrey, Tom, Da Rocha, Joana, Griffith, Renate, Knapp, Stefan, Bates, David O., Morris, Jonathan C. |
|---|---|
| Format: | Article |
| Published: |
American Chemical Society
2017
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| Online Access: | https://eprints.nottingham.ac.uk/40843/ |
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